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https://doi.org/10.1515/acph-2015-0022

Synthesis of pyranopyrazolo N-glycoside and pyrazolopyranopyrimidine C-glycoside derivatives as promising antitumor and antimicrobial agents

HEND N. HAFEZ ; Al-Imam Mohammad Ibn Saud Islamic University (IMSIU), Faculty of Science, Department of Chemistry, P.O. Box 90950, Riyadh 11623, Kingdom of Saudi Arabia; Photochemistry Department (Heterocyclic and Nucleosides Unit), National Research Centre, Cairo, Egypt
ABDEL-RHMAN B. A. EL-GAZZAR ; Al-Imam Mohammad Ibn Saud Islamic University (IMSIU), Faculty of Science, Department of Chemistry, P.O. Box 90950, Riyadh 11623, Kingdom of Saudi Arabia; Photochemistry Department (Heterocyclic and Nucleosides Unit), National Research Centre, Cairo, Egypt


Puni tekst: engleski pdf 456 Kb

str. 215-233

preuzimanja: 518

citiraj


Sažetak

As a part of systematic investigation of the synthesis and biological activities of pyrazole analogues linked to various heterocyclic systems, a new series of pyrazolo-N- nucleoside derivatives, pyrazolopyranopyrimidine and C-glycoside of pyrazolopyranotriazolo-pyrimidine derivatives was synthesized through the reaction of the key intermediate 6-amino-3-methyl-4-(substituted-phenyl)-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile (3a, b) with different reagents. Structures of the newly synthesized compounds were elucidated by elemental microanalysis and spectroscopic methods. The compounds were subjected to in vitro antitumor evaluation using the MTT assay. N-(β-D-ribofuranosyl)- and N-(β-D-xylofuranosyl)-6{[(1E)-4-chlorophenyl)-methylene]amino}4-(4-florophenyl)-3-methyl-1,4-dihydropyrano[2,3-c]-pyrazole-5-carbonitrile (6a, b) were the most active compounds against three human cancer cell lines. Also, most of the newly synthesized compounds exhibited high activity towards Gram-negative and Gram-positive bacteria. Compound 6a exhibited excellent activity towards bacteria compared to ofloxacine as the reference drug.

Ključne riječi

N-nucleoside of pyranopyrazole; C-glycoside of pyrazolopyranotriazolopyrimidine; anticancer activity; antimicrobial activity

Hrčak ID:

134865

URI

https://hrcak.srce.hr/134865

Datum izdavanja:

30.9.2015.

Posjeta: 1.289 *